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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01422044
Other study ID # 402/2009BO2-1
Secondary ID
Status Completed
Phase N/A
First received July 19, 2011
Last updated February 5, 2014
Start date September 2009
Est. completion date January 2014

Study information

Verified date February 2014
Source Thebiosignals.com
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Committee
Study type Observational

Clinical Trial Summary

The purpose of this study is to test the prognostic value of autonomic markers in patients with aortic stenosis.


Description:

Autonomic function will be assessed by presence of severe autonomic failure (defined by combination of abnormal heart rate turbulence and deceleration capacity).

Autonomic function will also be assessed by respiration and repolarization abnormalities.


Recruitment information / eligibility

Status Completed
Enrollment 423
Est. completion date January 2014
Est. primary completion date January 2014
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Aortic valve area =1.5 qcm or mean aortic gradient =25mmHg

Exclusion Criteria:

- life expectancy <1 year due to non-cardiac causes

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Locations

Country Name City State
Germany Medizinische Klinik III Tübingen

Sponsors (1)

Lead Sponsor Collaborator
Thebiosignals.com

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total mortality 2 years No
Secondary Cardiovascular mortality 2 years No
Secondary Combination of cardiovascular mortality and cardiac adverse events 2 years No
Secondary Correlation of presence of autonomic dysfunction with severity of aortic stenosis It will be assessed whether patients with cardiac autonomic dysfunction have more severe aortic stenosis.
Autonomic dysfunction will assumed to be present when patients suffer from "severe autonomic failure" (i.e. combination of abnormal Heart Rate Turbulence and Deceleration Capacity).
Severity of aortic stenosis will be assessed by clinical (symptoms, NYHA class), hemodynamic (mean aortic gradient, aortic valve area) and biochemical (Nt-BNP, high sensitive troponins) markers.
at time of cardiac catheterization, which will be performed at an expected average of 3 days after hospital admission No
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